Congenital pulmonary airway malformations (Q46283): Difference between revisions
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Doença causada por falha da estrutura brônquica em se desenvolver corretamente durante o período pré-natal. Esta doença pode se apresentar com desconforto respiratório grave no período neonatal, desconforto respiratório agudo ou infecção mais tarde na vida, ou pode ser assintomática. Esta doença pode ser diferenciada de outras lesões e do pulmão normal por projeções polipoides da mucosa, aumento do músculo liso e tecido elástico dentro das paredes dos cistos, ausência de cartilagem no parênquima cístico, células secretoras de mucosa e ausência de inflamação. | |||
| description / en | description / en | ||
A disease caused by failure of the bronchial structure to correctly develop during the antenatal period. This disease may present with severe respiratory distress in the newborn period, acute respiratory distress or infection later in life, or may be asymptomatic. This disease can be distinguished from other lesions and normal lung by polypoid projections of the mucosa, an increase in smooth muscle and elastic tissue within the cyst walls, an absence of cartilage in the cystic parenchyma, mucous secreting cells, and the absence of inflammation. | |||
Revision as of 14:45, 13 August 2026
A disease caused by failure of the bronchial structure to correctly develop during the antenatal period. This disease may present with severe respiratory distress in the newborn period, acute respiratory distress or infection later in life, or may be asymptomatic. This disease can be distinguished from other lesions and normal lung by polypoid projections of the mucosa, an increase in smooth muscle and elastic tissue within the cyst walls, an absence of cartilage in the cystic parenchyma, mucous secreting cells, and the absence of inflammation.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LA75.4 |
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| English | Congenital pulmonary airway malformations |
A disease caused by failure of the bronchial structure to correctly develop during the antenatal period. This disease may present with severe respiratory distress in the newborn period, acute respiratory distress or infection later in life, or may be asymptomatic. This disease can be distinguished from other lesions and normal lung by polypoid projections of the mucosa, an increase in smooth muscle and elastic tissue within the cyst walls, an absence of cartilage in the cystic parenchyma, mucous secreting cells, and the absence of inflammation. |
